Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750512
rs63750512
MAPT
0.020 GeneticVariation BEFREE Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome. 11193177

2000
dbSNP: rs63750512
rs63750512
MAPT
0.020 GeneticVariation BEFREE Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. 10604746

1999